CAS 62674-12-8

3,4-dichlorofuran-2(5H)-one

Description:

3,4-Dichlorofuran-2(5H)-one, with the CAS number 62674-12-8, is a heterocyclic organic compound characterized by its furan ring structure substituted with two chlorine atoms and a carbonyl group. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is known for its reactivity due to the presence of the carbonyl group, which can participate in various chemical reactions, including nucleophilic additions and cycloadditions. The dichloro substitutions enhance its electrophilic character, making it a useful intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Additionally, 3,4-dichlorofuran-2(5H)-one may exhibit biological activity, although specific biological properties would depend on the context of its use and the presence of other functional groups in related compounds. Safety precautions should be taken when handling this substance, as halogenated compounds can pose health risks and environmental concerns.

Formula: C₄H₂Cl₂O₂

InChI: InChI=1/C4H2Cl2O2/c5-2-1-8-4(7)3(2)6/h1H2

SMILES: C1C(=C(C(=O)O1)Cl)Cl

Synonyms:

• 2(5H)-furanone, 3,4-dichloro-

3,4-Dichloro-2(5H)-furanone

CAS: 62674-12-8

Formula: C₄H₂Cl₂O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 152.9635

Ref: IN-DA003IFW

3,4-Dichlorofuran-2(5H)-one

CAS: 62674-12-8

3,4-Dichlorofuran-2(5H)-one

Formula: C₄H₂Cl₂O₂

Purity: ≥95%

Color and Shape: off white to faint beige crystalline solid

Molecular weight: 152.96348g/mol

Ref: 54-OR31019

3,4-Dichloro-2,5-dihydrofuran-2-one

CAS: 62674-12-8

Purity: 98%

Molecular weight: 152.9600067

Ref: 10-F667533

3,4-Dichloro-2(5H)-furanone

CAS: 62674-12-8

3,4-Dichloro-2(5H)-furanone is a biologically active compound that has been shown to inhibit the growth of Listeria monocytogenes and typhimurium. It is a furanone analog with a chlorine substituent on the 2 position. The chemical structure of 3,4-Dichloro-2(5H)-furanone includes an oxygenated hydroxyl group at the 4 position, which is important for its bacteriostatic effects. The compound has been shown to be effective against multidrug resistant strains of bacteria such as methicillin resistant Staphylococcus aureus (MRSA). 3,4-Dichloro-2(5H)-furanone also has biological properties that are similar to those of other furanones found in nature. This molecule exhibits spectrometric properties typical of many furanones and can be easily reduced by sodium borohyd

Formula: C₄H₂Cl₂O₂

Purity: Min. 95%

Molecular weight: 152.96 g/mol

Ref: 3D-MCA67412